AI Article Synopsis

  • Double expressor lymphoma (DEL) is a serious form of diffuse large B cell lymphoma characterized by high levels of BCL2 and MYC proteins, and this report discusses a case involving a 64-year-old woman with DEL that developed from jejunum follicular lymphoma.
  • Imaging techniques, including 18F-FDG-PET scans and double balloon-assisted enteroscopy, revealed abnormal growths and accumulation of atypical lymphocytes in the jejunum, suggesting an aggressive transformation.
  • Genetic tests confirmed the presence of specific markers and chromosomal abnormalities typical of follicular lymphoma (FL), indicating that the patient’s prior indolent FL in the jejunum had transformed into DEL, underscoring the potential severity of gastrointestinal FL in some

Article Abstract

Double expressor lymphoma (DEL), defined as overexpression of BCL2 and MYC, is an aggressive subtype of diffuse large B cell lymphoma (DLBCL). Here we report a case of a 64-year-old female diagnosed with abdominal DEL transformed from jejunum follicular lymphoma (FL). 18F-fluorodeoxyglucose (FDG)-positron emission tomography showed diffuse accumulation of FDG into the peritoneum and small bowel wall. Double balloon-assisted enteroscopy revealed whitish submucosal tumors in the proximal jejunum. Aggregation of atypical lymphocytes positive for CD20, CD79a, and BCL2 was seen in the jejunal biopsy samples. These atypical lymphocytes were monoclonal since cell surface expression of Ig light chains was limited to κ chain by flow-cytometry. Thus, immunohistochemical and flowcytometric analyses data were consistent with FL of the jejunum. Neoplastic lymphocytes obtained from ascites were positive for CD10, CD20, CD79a, BCL2, and BCL6. Fluorescence hybridization (FISH) showed formation of fusion gene and extra copies of , the former of which is a characteristic chromosomal abnormality of FL. These genetic alterations and protein expression profiles of ascitic fluid cells were consistent with those of DEL transformed from FL. Given that a significant population of patients with indolent FL of the gastrointestinal tract developed into aggressive DLBCL, it is likely that primary FL of the jejunum transformed into the abdominal aggressive DEL in this case. This case is unique in that concurrent occurrence of FL and DEL was confirmed by immunohistochemical and FISH analyses and that abdominal DEL transformed from jejunal FL was highly suspected.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187768PMC
http://dx.doi.org/10.3389/fonc.2021.656219DOI Listing

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